Drugplain

NDC 71335-0845-1

Olmesartan Medoxomil and Hydrochlorothiazide 12.5 mg/1

Olmesartan Medoxomil and Hydrochlorothiazide · TABLET, FILM COATED

No Recall History

Olmesartan Medoxomil and Hydrochlorothiazide is a tablet, film coated containing olmesartan medoxomil and hydrochlorothiazide at a strength of 12.5 mg/1. Manufactured by Bryant Ranch Prepack.

Key Facts

Brand Name
Olmesartan Medoxomil and Hydrochlorothiazide
Generic Name
Olmesartan Medoxomil and Hydrochlorothiazide
NDC Code (Package)
71335-0845-1
NDC Code (Product)
71335-0845
Manufacturer
Bryant Ranch Prepack
Strength
12.5 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA205391
Drug Class
Thiazide Diuretic [EPC]
Marketing Start
04/24/2017

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.